Cas 216072-35-4,5-[4-(4-Chloro-phenyl)-3-pyrrol-1-yl-5,6,7,8-tetrahydro-thieno[2,3-b]quinolin-2-yl]-3H-[1,3,4]oxadiazole-2-thione

216072-35-4

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Basic information

Product Name: 5-[4-(4-Chloro-phenyl)-3-pyrrol-1-yl-5,6,7,8-tetrahydro-thieno[2,3-b]quinolin-2-yl]-3H-[1,3,4]oxadiazole-2-thione
Synonyms: 5-[4-(4-Chloro-phenyl)-3-pyrrol-1-yl-5,6,7,8-tetrahydro-thieno[2,3-b]quinolin-2-yl]-3H-[1,3,4]oxadiazole-2-thione
CAS NO:216072-35-4
Molecular Formula:
Molecular Weight: 464.999
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 5-[4-(4-Chloro-phenyl)-3-pyrrol-1-yl-5,6,7,8-tetrahydro-thieno[2,3-b]quinolin-2-yl]-3H-[1,3,4]oxadiazole-2-thione(CAS DataBase Reference)
NIST Chemistry Reference: 5-[4-(4-Chloro-phenyl)-3-pyrrol-1-yl-5,6,7,8-tetrahydro-thieno[2,3-b]quinolin-2-yl]-3H-[1,3,4]oxadiazole-2-thione(216072-35-4)
EPA Substance Registry System: 5-[4-(4-Chloro-phenyl)-3-pyrrol-1-yl-5,6,7,8-tetrahydro-thieno[2,3-b]quinolin-2-yl]-3H-[1,3,4]oxadiazole-2-thione(216072-35-4)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 216072-35-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 216072-35-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,6,0,7 and 2 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 216072-35:
(8*2)+(7*1)+(6*6)+(5*0)+(4*7)+(3*2)+(2*3)+(1*5)=104
104 % 10 = 4
So 216072-35-4 is a valid CAS Registry Number.

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216072-35-4Relevant academic research and scientific papers

Synthesis and antimicrobial activities of some new pyrrolylthieno[2,3- b]quinoline derivatives

Geies,Bakhite,El-Kashef

, p. 686 - 690 (2007/10/03)

2-Acetyl-4-(p-chlorophenyl)-3-(1-pyrroyl)-5,6,7,8-tetrahydrothieno[2,3- b]quinoline (4a) and its corresponding 2-carbohydrazide derivative 5 were prepared and used as key intermediates in the synthesis of the title compounds. Some of the synthesized compounds were screened for their antibacterial and antifungal activities.

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